Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration

• Published in: International journal of molecular sciences Vol. 23; no. 17; p. 9524
• Main Authors: Diaw, Sokhna Haissatou, Ganos, Christos, Zittel, Simone, Plötze-Martin, Kirstin, Kulikovskaja, Leonora, Vos, Melissa, Westenberger, Ana, Rakovic, Aleksandar, Lohmann, Katja, Dulovic-Mahlow, Marija
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23.08.2022; MDPI
• Subjects: Accumulation; Alzheimer's disease; Apoptosis; Atrophy; Autophagy; Autophagy - genetics; Basal ganglia; BPAN; Brain; Brain - metabolism; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cell culture; Cell cycle; Cell death; Central nervous system diseases; Cerebellum; Dystonia; Enzymes; Female; Females; ferritinophagy; Ferroptosis; Ferroptosis - genetics; Fibroblasts; Gait; Gene expression; Humans; Immunoblotting; Immunofluorescence; Iron; Iron - metabolism; Magnetic Resonance Imaging; Markers; Mitochondria; Mutants; Mutation; NCOA4; Neurodegeneration; Neurodegenerative Diseases - genetics; Nutrient deficiency; Parkinson's disease; Pathogenicity; Patients; Proteins; Signal transduction; Spasticity; WDR45; autophagy; ferroptosis; BPAN; GPX4; GBA; NCOA4; ferritinophagy; WDR45
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23179524

Beta-propeller protein-associated neurodegeneration (BPAN) is a subtype of neurodegeneration with brain iron accumulation (NBIA) caused by loss-of-function variants in WDR45. The underlying mechanism of iron accumulation in WDR45 deficiency remains elusive. We established a primary skin fibroblast culture of a new BPAN patient with a missense variant p.(Asn61Lys) in WDR45 (NM_007075.3: c.183C>A). The female patient has generalized dystonia, anarthria, parkinsonism, spasticity, stereotypies, and a distinctive cranial MRI with generalized brain atrophy, predominantly of the cerebellum. For the functional characterization of this variant and to provide a molecular link of WDR45 and iron accumulation, we looked for disease- and variant-related changes in the patient’s fibroblasts by qPCR, immunoblotting and immunofluorescence comparing to three controls and a previously reported WDR45 patient. We demonstrated molecular changes in mutant cells comprising an impaired mitochondrial network, decreased levels of lysosomal proteins and enzymes, and altered autophagy, confirming the pathogenicity of the variant. Compared to increased levels of the ferritinophagy marker Nuclear Coactivator 4 (NCOA4) in control cells upon iron treatment, patients’ cells revealed unchanged NCOA4 protein levels, indicating disturbed ferritinophagy. Additionally, we observed abnormal protein levels of markers of the iron-dependent cell death ferroptosis in patients’ cells. Altogether, our data suggests that WDR45 deficiency affects ferritinophagy and ferroptosis, consequentially disturbing iron recycling.